Product NDC: | 0603-1587 |
Proprietary Name: | Promethazine VC |
Non Proprietary Name: | Promethazinehydrochloride and phenylephrine hydrochloride |
Active Ingredient(s): | 5; 6.25 mg/5mL; mg/5mL & nbsp; Promethazinehydrochloride and phenylephrine hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | SYRUP |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0603-1587 |
Labeler Name: | Qualitest Pharmaceuticals |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040654 |
Marketing Category: | ANDA |
Start Marketing Date: | 20061207 |
Package NDC: | 0603-1587-58 |
Package Description: | 473 mL in 1 BOTTLE (0603-1587-58) |
NDC Code | 0603-1587-58 |
Proprietary Name | Promethazine VC |
Package Description | 473 mL in 1 BOTTLE (0603-1587-58) |
Product NDC | 0603-1587 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Promethazinehydrochloride and phenylephrine hydrochloride |
Dosage Form Name | SYRUP |
Route Name | ORAL |
Start Marketing Date | 20061207 |
Marketing Category Name | ANDA |
Labeler Name | Qualitest Pharmaceuticals |
Substance Name | PHENYLEPHRINE HYDROCHLORIDE; PROMETHAZINE HYDROCHLORIDE |
Strength Number | 5; 6.25 |
Strength Unit | mg/5mL; mg/5mL |
Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |